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Tricellulin antibody (AA 200-300)
MARVELD2
Reactivity: Human
WB
Host: Rabbit
Polyclonal
unconjugated
Product Details anti-Tricellulin Antibody
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Target
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Tricellulin (MARVELD2)
Binding Specificity
All epitopes for Tricellulin antibodies
AA 200-300
Reactivity
All reactivities for Tricellulin antibodies
Human
Host
All hosts for Tricellulin antibodies
Rabbit
Clonality
All clonalities for Tricellulin antibodies
Polyclonal
Conjugate
All conjugates for Tricellulin antibodies
This Tricellulin antibody is un-conjugated
Application
All applications for Tricellulin antibodies
Western Blotting (WB)
Sequence
ELLLGAGVFA CVTAYIHKDS EWYNLFGYSQ PYGMGGVGGL GSMYGGYYYT GPKTPFVLVV AGLAWITTII ILVLGMSMYY RTILLDSNWW PLTEFGINVA L
Cross-Reactivity
Human, Mouse, Rat
Characteristics
Polyclonal Antibodies
Immunogen
A synthetic peptide corresponding to a sequence within amino acids 200-300 of human MARVELD2 (NP_001033692.2).
Isotype
IgG
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Discover our top product MARVELD2 Primary Antibody
Alternatives
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Application Details
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Application Notes
WB,1:500 - 1:2000
Restrictions
For Research Use only
Handling
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Format
Liquid
Buffer
PBS with 0.02 % sodium azide,50 % glycerol, pH 7.3.
Preservative
Sodium azide
Precaution of Use
This product contains Sodium azide: a POISONOUS AND HAZARDOUS SUBSTANCE which should be handled by trained staff only.
Storage
-20 °C
Storage Comment
Store at -20°C. Avoid freeze / thaw cycles.
Target Details for Tricellulin
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Target
Tricellulin (MARVELD2)
Alternative Name
MARVELD2 (MARVELD2 Products )
Synonyms
Mrvldc2 antibody, BC003296 antibody, MARVD2 antibody, Tric antibody, Trica antibody, Tricb antibody, Tricc antibody, DFNB49 antibody, MRVLDC2 antibody, MARVEL domain containing 2 antibody, MARVEL (membrane-associating) domain containing 2 antibody, Marveld2 antibody, MARVELD2 antibody
Background
The protein encoded by this gene is a membrane protein found at the tight junctions between epithelial cells. The encoded protein helps establish epithelial barriers such as those in the organ of Corti, where these barriers are required for normal hearing. Defects in this gene are a cause of deafness autosomal recessive type 49 (DFNB49). Two transcript variants encoding different isoforms have been found for this gene.,MARVELD2,DFNB49,MARVD2,MRVLDC2,Tric,Signal Transduction,Cell Biology & Developmental Biology,Cell Adhesion,Tight Junctions,Cytoskeleton,MARVELD2
Molecular Weight
51 kDa/62 kDa/64 kDa
Gene ID
153562
UniProt
Q8N4S9
Pathways
Sensory Perception of Sound , Cell-Cell Junction Organization
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